Megakaryocytes Internalize and Are Activated by Immune Complexes
BACKGROUND: Receptors that bind antibodies are essential for protective adaptive immune responses against antibody-opsonized pathogens, yet their engagement by antibody-autoantigen complexes can drive chronic inflammation in autoimmune diseases. Megakaryocytes, the precursor cells of platelets, express such receptors. However, their response to immunoglobulin G antibodies remains unclear. METHODS: We used both systemic lupus erythematosus and COVID-19 as relevant examples of autoimmune and infection-driven contexts in which antibodies are involved to characterize human and mouse megakaryocyte responses. RESULTS: We found that megakaryocytes internalized immune complexes composed of autoantigens or SARS-CoV-2. In both human and mouse megakaryocytes, immune complexes triggered the release of chemokines and procoagulant extracellular vesicles. This process required FcγRIIA engagement, downstream Syk (spleen tyrosine kinase) signaling, and protein translation. A detailed analysis revealed that megakaryocyte-derived extracellular vesicles did not contain organelles and were largely indistinguishable from a subset of small-sized extracellular vesicles released by activated platelets. In FcγRIIA-transgenic mice, we analyzed megakaryocytes in both the bone marrow and lungs in a lupus model, whereas megakaryocytes were examined in the lungs in a COVID-19 model. In all cases, immunoglobulins were detected in close proximity to FcγRIIA-expressing megakaryocytes. Notably, the chemokine CXCL2 was increased in FcγRIIA-expressing mice under disease conditions. Tissue spatial analysis revealed that CXCL2 predominantly localized to megakaryocytes, supporting these cells as a major source. Furthermore, SARS-CoV-2 stimulated megakaryocytes to release CXCL2 only in the presence of IgG from SARS-CoV-2 immune individuals, and this response was strictly dependent on FcγRIIA expression. CONCLUSIONS: These findings suggest that megakaryocytes contribute to adaptive immune responses through FcγRIIA-mediated signaling.
Authors
- Bogdan I. Florea (ORCID: https://orcid.org/0000-0001-7114-2266)
- Florian Tupin
- Isabelle Dubuc (ORCID: https://orcid.org/0000-0003-3432-1980)
- Isabelle Allaeys (ORCID: https://orcid.org/0000-0003-4697-046X)
- ALBERTO D. ANDRADE (ORCID: https://orcid.org/0000-0001-9724-4164)
- Éric Boilard (ORCID: https://orcid.org/0000-0001-6319-6432)
- Alain Brisson (ORCID: https://orcid.org/0000-0003-0342-352X)
- Yaqiu Sang (ORCID: https://orcid.org/0000-0001-5147-989X)
- Florian Puhm (ORCID: https://orcid.org/0000-0001-5699-6626)
- Étienne Doré (ORCID: https://orcid.org/0000-0002-2347-5012)
- Eleonora Petito (ORCID: https://orcid.org/0000-0003-4921-8687)
- Loredana Bury (ORCID: https://orcid.org/0000-0003-0333-0948)
- Alisa S. Wolberg (ORCID: https://orcid.org/0000-0002-2845-2303)
- Marie‐Josée Hébert (ORCID: https://orcid.org/0000-0002-6234-682X)
- Patrick Trépanier (ORCID: https://orcid.org/0000-0002-8645-6230)
- Paul R. Fortin (ORCID: https://orcid.org/0000-0002-7278-2596)
- A. Valance Washington (ORCID: https://orcid.org/0000-0002-3458-1822)
- Mélanie Dieudé (ORCID: https://orcid.org/0000-0002-9300-4232)
- Louis Flamand (ORCID: https://orcid.org/0000-0001-5010-4586)
- Myriam Vaillancourt
- Yotis Senis
Institutions
- University of North Carolina at Chapel Hill (US)
- Centre National de la Recherche Scientifique (FR)
- Héma-Québec (CA)
- University of North Carolina Health Care (US)
- Université de Bordeaux (FR)
- Oakland University (US)
- University of Perugia (IT)
- Netherlands Metabolomics Centre (NL)
- Institut de Neurosciences de la Timone (FR)
- Centre hospitalier de l'Université Laval (CA)
- Centre Hospitalier de l’Université de Montréal (CA)
- Institut Polytechnique de Bordeaux (FR)
- Université Laval (CA)
Publication Details
- Journal
- Circulation Research
- Published
- 2026-06-16
- DOI
- https://doi.org/10.1161/circresaha.125.327999
- Primary Topic
- Systemic Lupus Erythematosus Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00